Canonical Allele Identifier: CA1748625384

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753920G= , CM000669.2:g.142753920G= GRCh38
NC_000007.13:g.142461771G= , CM000669.1:g.142461771G= GRCh37
NC_000007.12:g.142141345G= NCBI36
NG_008307.3:g.9437G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32734G= (TRBC1) ENSP00000482915.1:n.370+32734G=
ENST00000612126.4:c.591+1353G= (PRSS1) ENSP00000479959.1:n.591+1353G=
ENST00000633114.1:c.321+2026G= (PRSS2) ENSP00000487822.1:n.321+2026G=
ENST00000634019.1:c.82+5129G= (PRSS2) ENSP00000488594.1:n.82+5129G=